Early response assessment of glioma patients to definitive chemoradiotherapy using chemical exchange saturation transfer imaging at 7 T

Background Patients with newly diagnosed inoperable glioma receive chemoradiotherapy (CRT). Standard Response Assessment in Neuro‐Oncology (RANO) takes a minimum of 4 weeks after the end of treatment. Purpose/Hypothesis To investigate whether chemical exchange saturation transfer (CEST) MRI enables...

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Veröffentlicht in:Journal of magnetic resonance imaging 2019-10, Vol.50 (4), p.1268-1277
Hauptverfasser: Meissner, Jan‐Eric, Korzowski, Andreas, Regnery, Sebastian, Goerke, Steffen, Breitling, Johannes, Floca, Ralf Omar, Debus, Jürgen, Schlemmer, Heinz‐Peter, Ladd, Mark Edward, Bachert, Peter, Adeberg, Sebastian, Paech, Daniel
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container_end_page 1277
container_issue 4
container_start_page 1268
container_title Journal of magnetic resonance imaging
container_volume 50
creator Meissner, Jan‐Eric
Korzowski, Andreas
Regnery, Sebastian
Goerke, Steffen
Breitling, Johannes
Floca, Ralf Omar
Debus, Jürgen
Schlemmer, Heinz‐Peter
Ladd, Mark Edward
Bachert, Peter
Adeberg, Sebastian
Paech, Daniel
description Background Patients with newly diagnosed inoperable glioma receive chemoradiotherapy (CRT). Standard Response Assessment in Neuro‐Oncology (RANO) takes a minimum of 4 weeks after the end of treatment. Purpose/Hypothesis To investigate whether chemical exchange saturation transfer (CEST) MRI enables earlier assessment of response to CRT in glioma patients. Study Type Longitudinal prospective study. Population Twelve brain tumor patients who underwent definitive CRT were included in this study. Three longitudinal CEST MRI measurements were performed for each patient at 7T: first before, second immediately after completion of CRT, and a third measurement as a 6‐week follow‐up. Field Strength/Sequence Conventional MRI (contrast‐enhanced, T2w and diffusion‐weighted imaging) at 3T and T2w and CEST MRI at 7T was performed for all patients. Assessment The mean relaxation‐compensated relayed nuclear‐Overhauser‐effect CEST signal (rNOE) and the mean downfield‐rNOE‐suppressed amide proton transfer (dns‐APT) CEST signal were investigated. Additionally, choline‐to‐N‐acetyl‐aspartate ratios (Cho/NAA) were evaluated using single‐voxel 1H‐MRS in six of these patients. Performance of obtained contrasts was analyzed in assessing treatment response as classified according to the updated RANO criteria. Statistical Test Unpaired Student's t‐test. Results The rNOE signal significantly separated stable and progressive disease directly after the end of therapy (post‐treatment normalized to pre‐treatment mean ± SD: rNOEresponder = 1.090 ± 0.110, rNOEnon‐responder = 0.808 ± 0.155, P = 0.015). In contrast, no significant difference was observed between either group when assessing the normalized dns‐APT (dns‐APTresponder = 0.953 ± 0.384, dns‐APTnon‐responder = 0.972 ± 0.477, P = 0.95). In the smaller MRS subcohort, normalized Cho/NAA decreased in therapy responders (Cho/NAAresponder = 0.632 ± 0.007, Cho/NAAnon‐responder = 0.946 ± 0.124, P = 0.070). Data Conclusion rNOE mediated CEST imaging at 7T allowed for discrimination of responders and non‐responders immediately after the end of CRT, additionally supported by 1H‐MRS data. This is at least 4 weeks earlier than the standard clinical evaluation according to RANO. Therefore, CEST MRI may enable early response assessment in glioma patients. Level of Evidence: 1 Technical Efficacy Stage: 5 J. Magn. Reson. Imaging 2019;50:1268–1277.
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Standard Response Assessment in Neuro‐Oncology (RANO) takes a minimum of 4 weeks after the end of treatment. Purpose/Hypothesis To investigate whether chemical exchange saturation transfer (CEST) MRI enables earlier assessment of response to CRT in glioma patients. Study Type Longitudinal prospective study. Population Twelve brain tumor patients who underwent definitive CRT were included in this study. Three longitudinal CEST MRI measurements were performed for each patient at 7T: first before, second immediately after completion of CRT, and a third measurement as a 6‐week follow‐up. Field Strength/Sequence Conventional MRI (contrast‐enhanced, T2w and diffusion‐weighted imaging) at 3T and T2w and CEST MRI at 7T was performed for all patients. Assessment The mean relaxation‐compensated relayed nuclear‐Overhauser‐effect CEST signal (rNOE) and the mean downfield‐rNOE‐suppressed amide proton transfer (dns‐APT) CEST signal were investigated. Additionally, choline‐to‐N‐acetyl‐aspartate ratios (Cho/NAA) were evaluated using single‐voxel 1H‐MRS in six of these patients. Performance of obtained contrasts was analyzed in assessing treatment response as classified according to the updated RANO criteria. Statistical Test Unpaired Student's t‐test. Results The rNOE signal significantly separated stable and progressive disease directly after the end of therapy (post‐treatment normalized to pre‐treatment mean ± SD: rNOEresponder = 1.090 ± 0.110, rNOEnon‐responder = 0.808 ± 0.155, P = 0.015). In contrast, no significant difference was observed between either group when assessing the normalized dns‐APT (dns‐APTresponder = 0.953 ± 0.384, dns‐APTnon‐responder = 0.972 ± 0.477, P = 0.95). In the smaller MRS subcohort, normalized Cho/NAA decreased in therapy responders (Cho/NAAresponder = 0.632 ± 0.007, Cho/NAAnon‐responder = 0.946 ± 0.124, P = 0.070). Data Conclusion rNOE mediated CEST imaging at 7T allowed for discrimination of responders and non‐responders immediately after the end of CRT, additionally supported by 1H‐MRS data. This is at least 4 weeks earlier than the standard clinical evaluation according to RANO. Therefore, CEST MRI may enable early response assessment in glioma patients. Level of Evidence: 1 Technical Efficacy Stage: 5 J. Magn. Reson. Imaging 2019;50:1268–1277.</description><identifier>ISSN: 1053-1807</identifier><identifier>EISSN: 1522-2586</identifier><identifier>DOI: 10.1002/jmri.26702</identifier><identifier>PMID: 30864193</identifier><language>eng</language><publisher>Hoboken, USA: John Wiley &amp; Sons, Inc</publisher><subject>1H MRS ; Brain cancer ; Brain tumors ; CEST‐MRI ; Chemoradiotherapy ; chemoradiotherapy response ; Chemotherapy ; Choline ; dns‐APT ; Exchanging ; Field strength ; Glioma ; Longitude ; Magnetic resonance imaging ; Medical imaging ; Neuroimaging ; Oncology ; Organic chemistry ; Patients ; Population studies ; Radiation therapy ; rNOE ; Saturation ; Statistical tests ; Therapy</subject><ispartof>Journal of magnetic resonance imaging, 2019-10, Vol.50 (4), p.1268-1277</ispartof><rights>2019 International Society for Magnetic Resonance in Medicine</rights><rights>2019 International Society for Magnetic Resonance in Medicine.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3572-a46fffb53d7e9b1ceda6799bced0f58371190ba20ed2f15addd7021cb247887f3</citedby><cites>FETCH-LOGICAL-c3572-a46fffb53d7e9b1ceda6799bced0f58371190ba20ed2f15addd7021cb247887f3</cites><orcidid>0000-0001-5755-6833</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fjmri.26702$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fjmri.26702$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,1427,27903,27904,45553,45554,46387,46811</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/30864193$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Meissner, Jan‐Eric</creatorcontrib><creatorcontrib>Korzowski, Andreas</creatorcontrib><creatorcontrib>Regnery, Sebastian</creatorcontrib><creatorcontrib>Goerke, Steffen</creatorcontrib><creatorcontrib>Breitling, Johannes</creatorcontrib><creatorcontrib>Floca, Ralf Omar</creatorcontrib><creatorcontrib>Debus, Jürgen</creatorcontrib><creatorcontrib>Schlemmer, Heinz‐Peter</creatorcontrib><creatorcontrib>Ladd, Mark Edward</creatorcontrib><creatorcontrib>Bachert, Peter</creatorcontrib><creatorcontrib>Adeberg, Sebastian</creatorcontrib><creatorcontrib>Paech, Daniel</creatorcontrib><title>Early response assessment of glioma patients to definitive chemoradiotherapy using chemical exchange saturation transfer imaging at 7 T</title><title>Journal of magnetic resonance imaging</title><addtitle>J Magn Reson Imaging</addtitle><description>Background Patients with newly diagnosed inoperable glioma receive chemoradiotherapy (CRT). Standard Response Assessment in Neuro‐Oncology (RANO) takes a minimum of 4 weeks after the end of treatment. Purpose/Hypothesis To investigate whether chemical exchange saturation transfer (CEST) MRI enables earlier assessment of response to CRT in glioma patients. Study Type Longitudinal prospective study. Population Twelve brain tumor patients who underwent definitive CRT were included in this study. Three longitudinal CEST MRI measurements were performed for each patient at 7T: first before, second immediately after completion of CRT, and a third measurement as a 6‐week follow‐up. Field Strength/Sequence Conventional MRI (contrast‐enhanced, T2w and diffusion‐weighted imaging) at 3T and T2w and CEST MRI at 7T was performed for all patients. Assessment The mean relaxation‐compensated relayed nuclear‐Overhauser‐effect CEST signal (rNOE) and the mean downfield‐rNOE‐suppressed amide proton transfer (dns‐APT) CEST signal were investigated. Additionally, choline‐to‐N‐acetyl‐aspartate ratios (Cho/NAA) were evaluated using single‐voxel 1H‐MRS in six of these patients. Performance of obtained contrasts was analyzed in assessing treatment response as classified according to the updated RANO criteria. Statistical Test Unpaired Student's t‐test. Results The rNOE signal significantly separated stable and progressive disease directly after the end of therapy (post‐treatment normalized to pre‐treatment mean ± SD: rNOEresponder = 1.090 ± 0.110, rNOEnon‐responder = 0.808 ± 0.155, P = 0.015). In contrast, no significant difference was observed between either group when assessing the normalized dns‐APT (dns‐APTresponder = 0.953 ± 0.384, dns‐APTnon‐responder = 0.972 ± 0.477, P = 0.95). In the smaller MRS subcohort, normalized Cho/NAA decreased in therapy responders (Cho/NAAresponder = 0.632 ± 0.007, Cho/NAAnon‐responder = 0.946 ± 0.124, P = 0.070). Data Conclusion rNOE mediated CEST imaging at 7T allowed for discrimination of responders and non‐responders immediately after the end of CRT, additionally supported by 1H‐MRS data. This is at least 4 weeks earlier than the standard clinical evaluation according to RANO. Therefore, CEST MRI may enable early response assessment in glioma patients. Level of Evidence: 1 Technical Efficacy Stage: 5 J. Magn. Reson. Imaging 2019;50:1268–1277.</description><subject>1H MRS</subject><subject>Brain cancer</subject><subject>Brain tumors</subject><subject>CEST‐MRI</subject><subject>Chemoradiotherapy</subject><subject>chemoradiotherapy response</subject><subject>Chemotherapy</subject><subject>Choline</subject><subject>dns‐APT</subject><subject>Exchanging</subject><subject>Field strength</subject><subject>Glioma</subject><subject>Longitude</subject><subject>Magnetic resonance imaging</subject><subject>Medical imaging</subject><subject>Neuroimaging</subject><subject>Oncology</subject><subject>Organic chemistry</subject><subject>Patients</subject><subject>Population studies</subject><subject>Radiation therapy</subject><subject>rNOE</subject><subject>Saturation</subject><subject>Statistical tests</subject><subject>Therapy</subject><issn>1053-1807</issn><issn>1522-2586</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><recordid>eNp9kMFO3DAQQK0KVCjtpR-ALHGrFLCddRwfK7S0VCAkRM_RJB7vepXEqe0A-wX97XpZ6JGTR6OnN9Yj5Ctn55wxcbEZgjsXlWLiAznmUohCyLo6yDOTZcFrpo7Ipxg3jDGtF_IjOSpZXS24Lo_J3yWEfksDxsmPESnEiDEOOCbqLV31zg9AJ0gubyJNnhq0bnTJPSLt1jj4AMb5tMYA05bO0Y2rl73roKf43K1hXCGNkOaQJX6kKcAYLQbqBljtaEhU0YfP5NBCH_HL63tCfl8tHy5_Fjd3P64vv98UXSmVKGBRWWtbWRqFuuUdGqiU1m0emJV1qTjXrAXB0AjLJRhjchbetWKh6lrZ8oSc7b1T8H9mjKnZ-DmM-WQjhOZcKqV0pr7tqS74GAPaZgr5v2HbcNbsmje75s1L8wyfvirndkDzH32LnAG-B55cj9t3VM2v2_vrvfQfewSP5Q</recordid><startdate>201910</startdate><enddate>201910</enddate><creator>Meissner, Jan‐Eric</creator><creator>Korzowski, Andreas</creator><creator>Regnery, Sebastian</creator><creator>Goerke, Steffen</creator><creator>Breitling, Johannes</creator><creator>Floca, Ralf Omar</creator><creator>Debus, Jürgen</creator><creator>Schlemmer, Heinz‐Peter</creator><creator>Ladd, Mark Edward</creator><creator>Bachert, Peter</creator><creator>Adeberg, Sebastian</creator><creator>Paech, Daniel</creator><general>John Wiley &amp; Sons, Inc</general><general>Wiley Subscription Services, Inc</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QO</scope><scope>7TK</scope><scope>8FD</scope><scope>FR3</scope><scope>K9.</scope><scope>P64</scope><orcidid>https://orcid.org/0000-0001-5755-6833</orcidid></search><sort><creationdate>201910</creationdate><title>Early response assessment of glioma patients to definitive chemoradiotherapy using chemical exchange saturation transfer imaging at 7 T</title><author>Meissner, Jan‐Eric ; Korzowski, Andreas ; Regnery, Sebastian ; Goerke, Steffen ; Breitling, Johannes ; Floca, Ralf Omar ; Debus, Jürgen ; Schlemmer, Heinz‐Peter ; Ladd, Mark Edward ; Bachert, Peter ; Adeberg, Sebastian ; Paech, Daniel</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3572-a46fffb53d7e9b1ceda6799bced0f58371190ba20ed2f15addd7021cb247887f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>1H MRS</topic><topic>Brain cancer</topic><topic>Brain tumors</topic><topic>CEST‐MRI</topic><topic>Chemoradiotherapy</topic><topic>chemoradiotherapy response</topic><topic>Chemotherapy</topic><topic>Choline</topic><topic>dns‐APT</topic><topic>Exchanging</topic><topic>Field strength</topic><topic>Glioma</topic><topic>Longitude</topic><topic>Magnetic resonance imaging</topic><topic>Medical imaging</topic><topic>Neuroimaging</topic><topic>Oncology</topic><topic>Organic chemistry</topic><topic>Patients</topic><topic>Population studies</topic><topic>Radiation therapy</topic><topic>rNOE</topic><topic>Saturation</topic><topic>Statistical tests</topic><topic>Therapy</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Meissner, Jan‐Eric</creatorcontrib><creatorcontrib>Korzowski, Andreas</creatorcontrib><creatorcontrib>Regnery, Sebastian</creatorcontrib><creatorcontrib>Goerke, Steffen</creatorcontrib><creatorcontrib>Breitling, Johannes</creatorcontrib><creatorcontrib>Floca, Ralf Omar</creatorcontrib><creatorcontrib>Debus, Jürgen</creatorcontrib><creatorcontrib>Schlemmer, Heinz‐Peter</creatorcontrib><creatorcontrib>Ladd, Mark Edward</creatorcontrib><creatorcontrib>Bachert, Peter</creatorcontrib><creatorcontrib>Adeberg, Sebastian</creatorcontrib><creatorcontrib>Paech, Daniel</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>Biotechnology Research Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><jtitle>Journal of magnetic resonance imaging</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Meissner, Jan‐Eric</au><au>Korzowski, Andreas</au><au>Regnery, Sebastian</au><au>Goerke, Steffen</au><au>Breitling, Johannes</au><au>Floca, Ralf Omar</au><au>Debus, Jürgen</au><au>Schlemmer, Heinz‐Peter</au><au>Ladd, Mark Edward</au><au>Bachert, Peter</au><au>Adeberg, Sebastian</au><au>Paech, Daniel</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Early response assessment of glioma patients to definitive chemoradiotherapy using chemical exchange saturation transfer imaging at 7 T</atitle><jtitle>Journal of magnetic resonance imaging</jtitle><addtitle>J Magn Reson Imaging</addtitle><date>2019-10</date><risdate>2019</risdate><volume>50</volume><issue>4</issue><spage>1268</spage><epage>1277</epage><pages>1268-1277</pages><issn>1053-1807</issn><eissn>1522-2586</eissn><abstract>Background Patients with newly diagnosed inoperable glioma receive chemoradiotherapy (CRT). Standard Response Assessment in Neuro‐Oncology (RANO) takes a minimum of 4 weeks after the end of treatment. Purpose/Hypothesis To investigate whether chemical exchange saturation transfer (CEST) MRI enables earlier assessment of response to CRT in glioma patients. Study Type Longitudinal prospective study. Population Twelve brain tumor patients who underwent definitive CRT were included in this study. Three longitudinal CEST MRI measurements were performed for each patient at 7T: first before, second immediately after completion of CRT, and a third measurement as a 6‐week follow‐up. Field Strength/Sequence Conventional MRI (contrast‐enhanced, T2w and diffusion‐weighted imaging) at 3T and T2w and CEST MRI at 7T was performed for all patients. Assessment The mean relaxation‐compensated relayed nuclear‐Overhauser‐effect CEST signal (rNOE) and the mean downfield‐rNOE‐suppressed amide proton transfer (dns‐APT) CEST signal were investigated. Additionally, choline‐to‐N‐acetyl‐aspartate ratios (Cho/NAA) were evaluated using single‐voxel 1H‐MRS in six of these patients. Performance of obtained contrasts was analyzed in assessing treatment response as classified according to the updated RANO criteria. Statistical Test Unpaired Student's t‐test. Results The rNOE signal significantly separated stable and progressive disease directly after the end of therapy (post‐treatment normalized to pre‐treatment mean ± SD: rNOEresponder = 1.090 ± 0.110, rNOEnon‐responder = 0.808 ± 0.155, P = 0.015). In contrast, no significant difference was observed between either group when assessing the normalized dns‐APT (dns‐APTresponder = 0.953 ± 0.384, dns‐APTnon‐responder = 0.972 ± 0.477, P = 0.95). In the smaller MRS subcohort, normalized Cho/NAA decreased in therapy responders (Cho/NAAresponder = 0.632 ± 0.007, Cho/NAAnon‐responder = 0.946 ± 0.124, P = 0.070). Data Conclusion rNOE mediated CEST imaging at 7T allowed for discrimination of responders and non‐responders immediately after the end of CRT, additionally supported by 1H‐MRS data. This is at least 4 weeks earlier than the standard clinical evaluation according to RANO. Therefore, CEST MRI may enable early response assessment in glioma patients. Level of Evidence: 1 Technical Efficacy Stage: 5 J. Magn. Reson. Imaging 2019;50:1268–1277.</abstract><cop>Hoboken, USA</cop><pub>John Wiley &amp; Sons, Inc</pub><pmid>30864193</pmid><doi>10.1002/jmri.26702</doi><tpages>10</tpages><orcidid>https://orcid.org/0000-0001-5755-6833</orcidid></addata></record>
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subjects 1H MRS
Brain cancer
Brain tumors
CEST‐MRI
Chemoradiotherapy
chemoradiotherapy response
Chemotherapy
Choline
dns‐APT
Exchanging
Field strength
Glioma
Longitude
Magnetic resonance imaging
Medical imaging
Neuroimaging
Oncology
Organic chemistry
Patients
Population studies
Radiation therapy
rNOE
Saturation
Statistical tests
Therapy
title Early response assessment of glioma patients to definitive chemoradiotherapy using chemical exchange saturation transfer imaging at 7 T
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